Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Micro-minicircle gene therapy: Implications of size on fermentation, complexation, shearing resistance, and expression
Karolinska Institute, Sweden.
Karolinska Institute, Sweden.
RISE, SP – Sveriges Tekniska Forskningsinstitut, SP Kemi Material och Ytor.ORCID iD: 0000-0001-5894-7123
Karolinska Institute, Sweden.
Show others and affiliations
2014 (English)In: Molecular Therapy Nucleic Acids, E-ISSN 2162-2531, Vol. 2, article id e140Article in journal (Refereed) Published
Abstract [en]

The minicircle (MC), composed of eukaryotic sequences only, is an interesting approach to increase the safety and efficiency of plasmid-based vectors for gene therapy. In this paper, we investigate micro-MC (miMC) vectors encoding small regulatory RNA. We use a construct encoding a splice-correcting U7 small nuclear RNA, which results in a vector of 650 base pairs (bp), as compared to a conventional 3600 bp plasmid carrying the same expression cassette. Furthermore, we construct miMCs of varying sizes carrying different number of these cassettes. This allows us to evaluate how size influences production, supercoiling, stability and efficiency of the vector. We characterize coiling morphology by atomic force microscopy and measure the resistance to shearing forces caused by an injector device, the Biojector. We compare the behavior of miMCs and plasmids in vitro using lipofection and electroporation, as well as in vivo in mice. We here show that when the size of the miMC is reduced, the formation of dimers and trimers increases. There seems to be a lower size limit for efficient expression. We demonstrate that miMCs are more robust than plasmids when exposed to shearing forces, and that they show extended expression in vivo.

Place, publisher, year, edition, pages
2014. Vol. 2, article id e140
Keywords [en]
Nano, Pre-mRNA, RNA editing, RNA therapeutics
National Category
Natural Sciences
Identifiers
URN: urn:nbn:se:ri:diva-27324DOI: 10.1038/mtna.2013.67Scopus ID: 2-s2.0-84891787979OAI: oai:DiVA.org:ri-27324DiVA, id: diva2:1054328
Note

A3337

Available from: 2016-12-08 Created: 2016-12-08 Last updated: 2023-11-03Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textScopus

Authority records

Badal Tejedor, Maria

Search in DiVA

By author/editor
Badal Tejedor, Maria
By organisation
SP Kemi Material och Ytor
In the same journal
Molecular Therapy Nucleic Acids
Natural Sciences

Search outside of DiVA

GoogleGoogle Scholar

doi
urn-nbn

Altmetric score

doi
urn-nbn
Total: 64 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf